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Rituximab as treatment for refractory kidney transplant rejection
Author(s): Becker YT, Becker BN, Pirsch JD, Sollinger HW
Source: AMERICAN JOURNAL OF TRANSPLANTATION    Volume: 4    Issue: 6    Pages: 996-1001    Published: JUN 2004  
Times Cited: 104     References: 25     
Abstract: Recent studies have shown that a high density of CD 20+ cells are seen in patients who have steroid-resistant rejection episodes. Rituximab is a high-affinity CD-20 specific antibody that inhibits B-cell proliferation while inducing cellular apoptosis. Thus, it is a rational choice for therapy in transplantation to abrogate B-cell-mediated events.

Twenty-seven patients were diagnosed with biopsy-confirmed rejection manifested by thrombotic microangiopathy and/or endothelialitis between 2/99 and 2/02 at our institution. These individuals were treated with a single dose of rituximab, in addition to other therapies, in an effort to reverse their rejection episodes. Twenty-four received additional steroids while 22 of the 27 patients were also treated with plasmapheresis and antithymocyte globulin (ATG). Only three patients experienced graft loss not associated with patient death during the follow-up period (605+/-335.3 days). In the 24 successfully treated patients, the serum creatinine at the time of initiating rituximab therapy was 5.6+/-1.0 mg/dL and decreased to 0.95+/-0.7 mg/dL at discharge.

The addition of rituximab may improve outcomes in severe, steroid-resistant or antibody-mediated rejection episodes after kidney transplantation.

Document Type: Article
Language: English
Reprint Address: Becker, YT (reprint author), Univ Wisconsin, Dept Surg, Div Transplantat, Madison, WI 53706 USA
Addresses:
1. Univ Wisconsin, Dept Surg, Div Transplantat, Madison, WI 53706 USA
2. Univ Wisconsin, Dept Med, Div Nephrol, Madison, WI 53706 USA
Publisher: BLACKWELL MUNKSGAARD, 35 NORRE SOGADE, PO BOX 2148, DK-1016 COPENHAGEN, DENMARK
Subject Category: Surgery; Transplantation
IDS Number: 820VM
ISSN: 1600-6135
DOI: 10.1111/j.1600-6143.2004.00454.x
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